Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 2 de 2
Filter
Add filters








Language
Year range
1.
Rev. méd. Chile ; 131(9): 997-1002, sept. 2003.
Article in Spanish | LILACS | ID: lil-356013

ABSTRACT

BACKGROUND: Hyperhomocysteinemia is an independent cardiovascular risk factor that depends on folate and vitamin B12 nutrition. AIM: To measure homocysteine, folic acid and vitamin B12 serum levels in healthy children with and without a family history of cardiovascular disease. SUBJECTS AND METHODS: Forty children aged 6 to 15 years with a family history of cardiovascular disease, and 40 age and sex matched children without such history were studied. Serum homocysteine, folic acid and vitamin B12 were measured in a fasting blood sample. Homocysteine was measured by a fluorescence polarization immunoassay (FPIA), vitamin B12 by enzymatic microparticle assay, covered with intrinsic factor and folic acid by ionic capture, using commercial kits. RESULTS: Children with family history of cardiovascular disease had higher homocysteine levels than their counterparts without family history (7.9 +/- 3 and 5.8 +/- 2 mumol/l respectively, p < 0.03), but similar folic acid (5.2 +/- 1.8 and 5.5 +/- 1.4 pg/ml respectively) and vitamin B12 levels (431 +/- 213 and 445 +/- 209 ng/ml respectively). There was a negative and significant correlation between homocysteine and folic acid and vitamin B12 levels. CONCLUSIONS: Children with a family history of cardiovascular disease have higher levels of serum homocysteine than those without such history, despite having similar levels of folic acid and vitamin B12.


Subject(s)
Humans , Male , Female , Child , Adolescent , Cardiovascular Diseases/blood , Homocysteine/blood , Hyperhomocysteinemia , Folic Acid/blood , Cardiovascular Diseases/genetics , Risk Factors , Lipoproteins/blood , Lipids/blood , /blood
2.
Rev. chil. pediatr ; 54(5): 344-9, 1983.
Article in Spanish | LILACS | ID: lil-18157

ABSTRACT

Se presenta dos casos de ninos portadores de sindrome de Crigler Najjar. Su diagnostico ha sido confirmado por estudio enzimatico y de microscopia electronica. Se clasifican en tipo I y II de acuerdo con su respuesta al tratamiento con fenobarbital. Se revisan brevemente las hiperbilirrubinemias no hemoliticas congenitas destacando que a pesar del conocimiento actual queda aun mucho por investigar


Subject(s)
Infant, Newborn , Humans , Male , Crigler-Najjar Syndrome , Glucuronosyltransferase
SELECTION OF CITATIONS
SEARCH DETAIL